Guide Full Lindemann Drill

GUDID 08809918274044

Dental Implant Surgical Instrument - Drill

Ossvis Co., Ltd.

Fixture/appliance dental drill bit, reusable

• Primary Device ID: 08809918274044
• NIH Device Record Key: 321d4d00-f28a-452f-bb99-4c61161c503f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Full Lindemann Drill
• Version Model Number: HLD1807GF
• Company DUNS: 695365503
• Company Name: Ossvis Co., Ltd.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809918274044 [Primary]

FDA Product Code

• DZA: Drill, Dental, Intraoral

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[08809918274044]

Moist Heat or Steam Sterilization

[08809918274044]

Moist Heat or Steam Sterilization

[08809918274044]

Moist Heat or Steam Sterilization

[08809918274044]

Moist Heat or Steam Sterilization

[08809918274044]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [Guide Full Lindemann Drill]

• 08809918274082: Dental Implant Surgical Instrument - Drill
• 08809918274075: Dental Implant Surgical Instrument - Drill
• 08809918274068: Dental Implant Surgical Instrument - Drill
• 08809918274051: Dental Implant Surgical Instrument - Drill
• 08809918274044: Dental Implant Surgical Instrument - Drill